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Studying the effectiveness of ultrasound-guided caudal block for pain relief after femur fracture surgery with spinal anesthesia.

To Study the efficacy of ultrasound guided caudal block for post operative analgesia in patients undergoing femur fracture surgery under subarachnoid block - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/083840
Enrollment
70
Registered
2025-04-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: S729- Unspecified fracture of femur Health Condition 2: S729- Unspecified fracture of femur Health Condition 3: S729- Unspecified fracture of femur Health Condition 4: S729- Unspecified fracture of femur

Interventions

Intervention1: Caudal block: Ultrasound guided caudal block with 0.2% Ropivacaine 0.3-0.5 ml/kg in caudal epidural space Control Intervention1: Intravenous analgesia.: Alternative intravenous pain man

Sponsors

Mahatma Gandhi medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient scheduled for femur fracture surgeries under subarachnoid block. Patient with ASA grade I,II and III.

Exclusion criteria

Exclusion criteria: Subject s refusal to participate in the study Any bleeding disorder or patient on anticoagulants. Neurological deficits History of drug allergy. Local infection at the injection site. Patients on any sedatives or antipsychotics.

Design outcomes

Primary

MeasureTime frame
Assessment of pain using VAS ( visual analogue scale ) score at interval of 2hrs for 24hrs between the two groups. Group A : Ultrasound Guided caudal block group- 0.2% Ropivacaine 0.3-0.5ml/kg Group B : The alternative intravenous pain management group (Control group) Timepoint: 0,2nd hour, 4th hour, 6th hour, 8th hour, 10th hour, 12th hour, 14th hour, 16th hour, 18th hour, 20th hour, 22nd hour, 24th hour.

Secondary

MeasureTime frame
To assess the time of first rescue analgesia between the two groups. To assess & compare the total dose required in first 24 hour post- operatively in both patient groups. Timepoint: 0,2nd hour, 4th hour, 6th hour, 8th hour, 10th hour, 12th hour, 14th hour, 16th hour, 18th hour, 20th hour, 22nd hour, 24th hour.

Countries

India

Contacts

Public ContactDr Mangilal deganwa

Mahatma Gandhi medical college and hospital

mangilaldeganwa0606@gmail.com9871495240

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026